Treatment outcomes of subsequent-line Regorafenib in patients with advanced hepatocellular carcinoma
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Abstract
This retrospective combined with prospective descriptive study was conducted on 61 patients with advanced hepatocellular carcinoma treated with Regorafenib at K Hospital from August 2024 to April 2026. The objective response rate and disease control rate in the overall population were 3.3% and 18.0%, respectively. The median progression-free survival and overall survival calculated from the initiation of Regorafenib were 3.0 and 6.4 months, respectively. Impaired liver function (Child-Pugh B/C) and severe portal vein tumor thrombus (Vp3/Vp4) were independent adverse prognostic factors for overall survival. The most common adverse event was hand-foot skin reaction (21.3%), with the majority being mild. For patients with hepatocellular carcinoma who progressed after previous systemic therapies, subsequent treatment with Regorafenib in a selected population with preserved liver function demonstrated a safety profile and improved overall survival in real-world clinical practice in Vietnam.
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Keywords
Hepatocellular carcinoma, Regorafenib, subsequent-line therapy, prognostic factors
References
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